Reference health
Applications of cyclometalation reaction five-membered ring products
174/174 checkable references clean · checked 2026-07-23
Every reference with a DOI in the deposited reference list resolved to a known work in Crossref or DataCite at the dated check, and none carried a retraction, withdrawal, or removal notice.
40 without a DOI — not checked. A reference deposited without a DOI is never matched by title or guessed at; it stays outside the checked set, and this line discloses that.
The 174 checked references that resolve
resolves10.1016/S0277-5387(00)88056-0
Cyclometallated complexes incorporating a heterocyclic donor atom; the interface of coordination chemistry and organometallic chemistry
resolves10.1021/cr00072a006
Cyclometalation of the platinum metals with nitrogen and alkyl, alkenyl, and benzyl carbon donors
resolves10.1070/RC1988v057n03ABEH003348
General Principles and Characteristics of Cyclopalladation Reactions
resolves10.1002/recl.19901091202
Reactions of cyclopalladated compounds and alkynes: New pathways for organic synthesis?
resolves10.1021/cr00100a004
Mechanisms of intramolecular activation of carbon-hydrogen bonds in transition-metal complexes
resolves10.1021/cr00039a006
Intramolecular Coordination in Organometallic Compounds of Groups 2, 12, and 13
resolves10.1016/j.ccr.2005.10.003
Ortho-metallated transition metal complexes derived from tertiary phosphine and arsine ligands
resolves10.1021/cr900279a
Cyclometalation Using d-Block Transition Metals: Fundamental Aspects and Recent Trends
resolves10.5059/yukigoseikyokaishi.71.588
Development and Application of Efficient Methods for Extension of ^|^pi;-Conjugated Systems by Catalytic Substitution Reactions via Chelation-Assisted Cleavage of Unreactive Aromatic Carbon Bonds
resolves10.1016/j.ccr.2009.01.013
Heavy metal organometallic electrophosphors derived from multi-component chromophores
resolves10.1039/b819943d
Functional metallophosphors for effective charge carrier injection/transport: new robust OLED materials with emerging applications
resolves10.1002/asia.201000928
New Design Tactics in OLEDs Using Functionalized 2‐Phenylpyridine‐Type Cyclometalates of Iridium(III) and Platinum(II)
resolves10.1016/j.jphotochemrev.2011.01.001
Recent progress and current challenges in phosphorescent white organic light-emitting diodes (WOLEDs)
resolves10.1002/ajoc.201402266
Recent Advances in Solution‐Processable Dendrimers for Highly Efficient Phosphorescent Organic Light‐Emitting Diodes (PHOLEDs)
resolves10.1016/j.jorganchem.2013.09.035
Red to near-infrared organometallic phosphorescent dyes for OLED applications
resolves10.1039/c3nj00170a
Small-molecular blue phosphorescent dyes for organic light-emitting devices
resolves10.1039/c3tc31953a
Recent design tactics for high performance white polymer light-emitting diodes
resolves10.1016/j.ccr.2012.08.023
Charge and energy transfers in functional metallophosphors and metallopolyynes
resolves10.1021/cr60320a001
Organometallic intramolecular-coordination compounds containing a nitrogen donor ligand
resolves10.1016/S0010-8545(00)82010-X
Organometallic intramolecular-coordination compounds. Recent aspects in the study of sulfur donor ligands
resolves10.1016/S0010-8545(00)80376-8
Organometallic intramolecular-coordination compounds containing a phosphorus donor ligand
resolves10.1016/S0010-8545(00)80526-3
Organometallic intramolecular-coordination compounds containing a cyclopentadienyl donor ligand
resolves10.1016/S0010-8545(00)80536-6
Organometallic intramolecular-coordination compounds containing an arsine donor ligand
resolves10.1016/0010-8545(83)80025-3
Organometallic intramolecular-coordination compounds containing a diolefin donor ligand
resolves10.1016/0010-8545(84)85010-9
Organometallic intramolecular-coordination compounds containing a π-allyl donor ligand
resolves10.1016/0010-8545(88)80022-5
Recent studies on organometallic intramolecular-coordination compounds
resolves10.1016/j.jorganchem.2007.02.036
Three types of reactions with intramolecular five-membered ring compounds in organic synthesis
resolves10.1002/aoc.1630
Carbonyl group‐containing organometallic intramolecular‐coordination five‐membered ring compounds
resolves10.1016/j.ccr.2014.07.019
Applications of five-membered ring products of cyclometalation reactions as anticancer agents
resolves10.1016/j.ccr.2015.08.009
Application of the five-membered ring blue light-emitting iridium products of cyclometalation reactions as OLEDs
resolves10.2174/1385272819666151022220954
Carbon Dioxide Utilization by the Five-Membered Ring Products of Cyclometalation Reactions
resolves10.4236/mrc.2016.53006
Applications of Cyclometalation Five-Membered Ring Products and Intermediates as Catalytic Agents
resolves10.2174/1385272820666160831142355
Application of the Five-Membered Ring Ruthenium Products of Cyclometalation Reactions for Manufacturing Dye-Sensitized Solar Cells
resolves10.1016/j.jorganchem.2016.09.008
Application of five-membered ring products of cyclometalation reactions as sensing materials in sensing devices
resolves10.1016/j.jorganchem.2017.04.010
Application of the five-membered ring products of cyclometalation reactions for hydrogen production
resolves10.1016/j.jorganchem.2017.07.035
Applications of six-membered ring products from cyclometalation reactions
resolves10.1016/S0022-328X(98)01065-1
Palladium catalyzed enantioselective rearrangement of allylic imidates to allylic amides
resolves10.1021/ol0271786
Catalytic Asymmetric Rearrangement of Allylic <i>N</i>-Aryl Trifluoroacetimidates. A Useful Method for Transforming Prochiral Allylic Alcohols to Chiral Allylic Amines
resolves10.1021/ja037086r
Catalytic Asymmetric Rearrangement of Allylic Trichloroacetimidates. A Practical Method for Preparing Allylic Amines and Congeners of High Enantiomeric Purity
resolves10.1021/om0493614
Synthesis of <i>tert</i>-Leucine-Derived Cobalt Oxazoline Palladacycles. Reversal of Palladation Diastereoselectivity and Application to the Asymmetric Rearrangement of <i>N</i>-Aryl Trifluoroacetimidates
resolves10.1002/anie.200454199
Cyclometalated Ruthenium(<scp>II</scp>) Complexes as Highly Active Transfer Hydrogenation Catalysts
resolves10.1021/ol047353d
Cycloruthenated Primary and Secondary Amines as Efficient Catalyst Precursors for Asymmetric Transfer Hydrogenation
resolves10.1002/anie.200502118
Ruthenium(<scp>II</scp>) Terdentate CNN Complexes: Superlative Catalysts for the Hydrogen‐Transfer Reduction of Ketones by Reversible Insertion of a Carbonyl Group into the RuH Bond
resolves10.1002/1521-3765(20020703)8:13<2968::AID-CHEM2968>3.0.CO;2-6
Novel Asymmetric Michael Addition of α-Cyanopropionates to Acrolein by the Use of a Bis(oxazolinyl)phenylstannane-Derived Rhodium(III) Complex as a Chiral Lewis Acid Catalyst
resolves10.1016/S0040-4039(97)01309-9
Synthesis and application of cationic 2,6-bis(2-oxazolinyl)phenylpalladium(II) complexes
resolves10.1021/om990710h
Cationic [2,6-Bis(2‘-oxazolinyl)phenyl]palladium(II) Complexes: Catalysts for the Asymmetric Michael Reaction
resolves10.1021/om0305162
Synthesis of 2,6-Bis(2-oxazolinyl)phenylplatinum(II) NCN Pincer Complexes by Direct Cyclometalation. Catalysts for Carbon−Carbon Bond Formation
resolves10.1039/a903573g
Iridium PCP pincer complexes: highly active and robust catalysts for novel homogeneous aliphatic dehydrogenations
resolves10.1021/ja0289200
Mechanism of Alkane Transfer-Dehydrogenation Catalyzed by a Pincer-Ligated Iridium Complex
resolves10.1039/b304357f
Novel synthesis of enamines by iridium-catalyzed dehydrogenation of tertiary aminesElectronic supplementary information (ESI) available: detailed experimental procedures and spectroscopic information. See http://www.rsc.org/suppdata/cc/b3/b304357f/
resolves10.5059/yukigoseikyokaishi.61.343
Chiral Transition Metal Lewis Acids Bearing Bis(oxazolinyl)phenyl (Phebox) as a Pincer Ligand: Synthesis and Application for the Asymmetric Reactions
resolves10.1016/S0040-4020(00)01049-8
Asymmetric hetero Diels–Alder reaction of Danishefsky's dienes and glyoxylates with chiral bis(oxazolinyl)phenylrhodium(III) aqua complexes, and its mechanistic studies
resolves10.1021/cr960118r
Cyclometalated Phosphine-Based Pincer Complexes: Mechanistic Insight in Catalysis, Coordination, and Bond Activation
resolves10.1021/om011011j
Formation of Fischer Carbene Complexes in Asymmetric Aldol-Type Condensation of an Isocyanide Component on Bis(oxazolinyl)phenylrhodium(III) Complexes with Aldehydes: Stereochemistry, Structural Characterization, and Mechanistic Studies
resolves10.1021/jo970044z
Cyclopropanation with Diazomethane and Bis(oxazoline)palladium(II) Complexes
resolves10.1021/om010018y
Bis(oxazolinyl)phenylrhodium(III) Aqua Complexes: Synthesis, Structure, Enantioselective Allylation of Aldehydes, and Mechanistic Studies
resolves10.1021/om049848c
Mechanism of the Methylene Transfer Reaction. C−C Activation and Reductive Elimination in One System. A DFT Study
resolves10.1021/om040061w
Carbon−Oxygen Bond Formation at Metal(IV) Centers: Reactivity of Palladium(II) and Platinum(II) Complexes of the [2,6-(Dimethylaminomethyl)phenyl-<i>N</i>,<i>C</i>,<i>N</i>]<sup>-</sup>(Pincer) Ligand toward Iodomethane and Dibenzoyl Peroxide; Structural Studies of M(II) and M(IV) Complexes
resolves10.1016/j.jorganchem.2005.03.031
An ionic liquid-tagged second generation Hoveyda–Grubbs ruthenium carbene complex as highly reactive and recyclable catalyst for ring-closing metathesis of di-, tri- and tetrasubstituted dienes
resolves10.1021/ja001179g
Efficient and Recyclable Monomeric and Dendritic Ru-Based Metathesis Catalysts
resolves10.1021/cr9002424
Ruthenium-Based Heterocyclic Carbene-Coordinated Olefin Metathesis Catalysts
resolves10.1002/1521-3773(20021115)41:22<4176::AID-ANIE4176>3.0.CO;2-U
Palladium-Catalyzed Coupling Reactions of Aryl Chlorides
resolves10.1021/om049001g
Synthesis and Characterization of<i>N</i>-Heterocyclic Carbene Phospha-Palladacycles and Their Properties in Heck Catalysis
resolves10.1016/S0022-328X(02)01727-8
Cross-coupling reactions with boronic acids in water catalysed by oxime-derived palladacycles
resolves10.1039/a806041j
Orthopalladated triaryl phosphite complexes as highly active catalysts in biaryl coupling reactions
resolves10.1021/om0492395
Catalytic Suzuki Coupling Reactions by Amido Phosphine Complexes of Palladium
resolves10.1002/chem.201103679
Providing Support in Favor of the Existence of a Pd<sup>II</sup>/Pd<sup>IV</sup> Catalytic Cycle in a Heck‐Type Reaction
resolves10.1016/j.jorganchem.2011.08.024
Dinuclear macrocyclic palladium complexes having pincer coordinating groups and their catalytic properties in Mizoroki–Heck reactions
resolves10.1039/c1sc00267h
One-step synthesis of composite vesicles: Direct polymerization and in situ over-oxidation of thiophene
resolves10.1039/c3sc21972k
A dinuclear cyclometalated gold(iii)–phosphine complex targeting thioredoxin reductase inhibits hepatocellular carcinoma in vivo
resolves10.1039/c001216e
Cyclometalated gold(iii) complexes with N-heterocyclic carbene ligands as topoisomerase I poisons
resolves10.1039/c1dt10322a
Library of second-generation cycloruthenated compounds and evaluation of their biological properties as potential anticancer drugs: Passing the nanomolar barrier
resolves10.1002/ejic.200800003
Isolation of an Intermediate in the Platination of <i>p</i>‐Nitroacetophenone 4‐Methylthiosemicarbazone: Potential Application as an Antitumor Drug
resolves10.1021/jm970520d
Novel Tetranuclear Orthometalated Complexes of Pd(II) and Pt(II) Derived from <i>p</i>-Isopropylbenzaldehyde Thiosemicarbazone with Cytotoxic Activity in <i>cis</i>-DDP Resistant Tumor Cell Lines. Interaction of These Complexes with DNA
resolves10.1002/(SICI)1099-0739(199812)12:12<809::AID-AOC754>3.0.CO;2-X
DNA binding andin vitro antileukemic activity of dimeric and tetrameric platinated complexes derived fromp-isopropylbenzaldehyde thiosemicarbazone
resolves10.1016/S0162-0134(99)00021-5
A cycloplatinated compound of p-isopropylbenzaldehyde thiosemicarbazone and its chloro-bridged derivative induce apoptosis in cis-DDP resistant cells which overexpress the H-ras oncogene
resolves10.1016/S0162-0134(99)00102-6
Synthesis and characterization of Pd(II) and Pt(II) complexes of -isopropylbenzaldehyde N-protected thiosemicarbazones. Cytotoxic activity against -transformed cells
resolves10.1016/j.ejmech.2012.06.002
Seven-membered cycloplatinated complexes as a new family of anticancer agents. X-ray characterization and preliminary biological studies
resolves10.1021/om800864f
Five- and Seven-Membered Metallacycles in [C,N,N′] and [C,N] Cycloplatinated Compounds
resolves10.1021/om030674t
Compound [PtPh<sub>2</sub>(SMe<sub>2</sub>)<sub>2</sub>] as a Versatile Metalating Agent in the Preparation of New Types of [C,N,N‘] Cyclometalated Platinum Compounds
resolves10.1021/om00054a031
Competition between intramolecular oxidative addition and ortho metalation in organoplatinum(II) compounds: activation of aryl-halogen bonds
resolves10.1016/j.jorganchem.2012.11.034
Cyclopalladated benzophenone imines: Synthesis, cytotoxicity against human breast adenocarcinoma cell lines and DNA interaction
resolves10.1021/ic201153d
Luminescent Cyclometalated Iridium(III) Polypyridine Di-2-picolylamine Complexes: Synthesis, Photophysics, Electrochemistry, Cation Binding, Cellular Internalization, and Cytotoxic Activity
resolves10.1002/chem.201000474
Modification of Luminescent Iridium(III) Polypyridine Complexes with Discrete Poly(ethylene glycol) (PEG) Pendants: Synthesis, Emissive Behavior, Intracellular Uptake, and PEGylation Properties
resolves10.1002/chem.201200979
Cyclometalated Iridium(III)–Polyamine Complexes with Intense and Long‐Lived Multicolor Phosphorescence: Synthesis, Crystal Structure, Photophysical Behavior, Cellular Uptake, and Transfection Properties
resolves10.1039/c2ra20967e
Iridium(iii) complexes as therapeutic and bioimaging reagents for cellular applications
resolves10.1016/j.biomaterials.2013.06.028
Mitochondria-targeting cyclometalated iridium(III)–PEG complexes with tunable photodynamic activity
resolves10.1021/jm010203d
Mononuclear Platinum(II) Complex with 2-Phenylpyridine Ligands Showing High Cytotoxicity against Mouse Sarcoma 180 Cells Acquiring High Cisplatin Resistance
resolves10.1016/S0162-0134(00)00211-7
Platinum (II) complex with cyclometalating 2-phenylpyridine ligand showing high cytotoxicity against cisplatin-resistant cell
resolves10.1021/om3006239
Organometallic Palladium Complexes with a Water-Soluble Iminophosphorane Ligand As Potential Anticancer Agents
resolves10.1021/om500001h
Cytotoxicity Studies of Cyclometallated Ruthenium(II) Compounds: New Applications for Ruthenium Dyes
resolves10.1002/anie.201602814
Cyclometalated Palladium(II) N‐Heterocyclic Carbene Complexes: Anticancer Agents for Potent In Vitro Cytotoxicity and In Vivo Tumor Growth Suppression
resolves10.1002/adma.200401373
New Dopant and Host Materials for Blue‐Light‐Emitting Phosphorescent Organic Electroluminescent Devices
resolves10.1021/ja034537z
Synthesis and Characterization of Facial and Meridional Tris-cyclometalated Iridium(III) Complexes
resolves10.1021/ic0008969
Synthesis and Characterization of Phosphorescent Cyclometalated Iridium Complexes
resolves10.1021/ja003693s
Highly Phosphorescent Bis-Cyclometalated Iridium Complexes: Synthesis, Photophysical Characterization, and Use in Organic Light Emitting Diodes
resolves10.1039/B406851C
Tuning iridium(
<scp>iii</scp>
) phenylpyridine complexes in the “almost blue” region
resolves10.1002/anie.200604733
Blue‐Emitting Heteroleptic Iridium(III) Complexes Suitable for High‐Efficiency Phosphorescent OLEDs
resolves10.1021/ic900607s
Authentic-Blue Phosphorescent Iridium(III) Complexes Bearing Both Hydride and Benzyl Diphenylphosphine; Control of the Emission Efficiency by Ligand Coordination Geometry
resolves10.1002/ejic.200900936
Synthesis and Photophysical Properties of Substituted Tris(phenylbenzimidazolinato) Ir<sup>III</sup> Carbene Complexes as a Blue Phosphorescent Material
resolves10.1002/adma.201102886
Wide‐Range Color Tuning of Iridium Biscarbene Complexes from Blue to Red by Different <i>N</i>⁁<i>N</i> Ligands: an Alternative Route for Adjusting the Emission Colors
resolves10.1021/ic500070s
Blue-Green Iridium(III) Emitter and Comprehensive Photophysical Elucidation of Heteroleptic Cyclometalated Iridium(III) Complexes
resolves10.1021/ic201899z
Effects of Fluorination on Iridium(III) Complex Phosphorescence: Magnetic Circular Dichroism and Relativistic Time-Dependent Density Functional Theory
resolves10.1021/om400770h
Effective Alkoxylation of Phosphorescent Heteroleptic Iridium(III) Compounds Bearing Fluorinated Bipyridine Ligands
resolves10.1021/ja903157e
High-Triplet-Energy Dendrons: Enhancing the Luminescence of Deep Blue Phosphorescent Iridium(III) Complexes
resolves10.1002/adma.201305733
Highly Efficient Organic Light‐Emitting Diodes with Phosphorescent Emitters Having High Quantum Yield and Horizontal Orientation of Transition Dipole Moments
resolves10.1016/j.ccr.2012.03.017
Recent developments in carbon dioxide utilization for the production of organic chemicals
resolves10.1002/chem.201102147
Visible‐Light‐Driven H<sub>2</sub> Generation from Water and CO<sub>2</sub> Conversion by Using a Zwitterionic Cyclometalated Iridium(III) Complex
resolves10.1021/ja109097z
Rhodium(I)-Catalyzed Direct Carboxylation of Arenes with CO<sub>2</sub> via Chelation-Assisted C−H Bond Activation
resolves10.1002/chem.201103992
Synthesis of PCP‐Supported Nickel Complexes and their Reactivity with Carbon Dioxide
resolves10.1021/ja00067a063
Conversion of light to electricity by cis-X2bis(2,2'-bipyridyl-4,4'-dicarboxylate)ruthenium(II) charge-transfer sensitizers (X = Cl-, Br-, I-, CN-, and SCN-) on nanocrystalline titanium dioxide electrodes
resolves10.1021/ic990916a
Acid−Base Equilibria of (2,2‘-Bipyridyl-4,4‘-dicarboxylic acid)ruthenium(II) Complexes and the Effect of Protonation on Charge-Transfer Sensitization of Nanocrystalline Titania
resolves10.1021/ja003299u
Engineering of Efficient Panchromatic Sensitizers for Nanocrystalline TiO<sub>2</sub>-Based Solar Cells
resolves10.1021/ic200872a
A New Class of Cyclometalated Ruthenium Sensitizers of the Type ĈN̂N for Efficient Dye-Sensitized Solar Cells
resolves10.1246/cl.130664
Cosensitization of Cyclometalated Ruthenium Complex and Organic Dyes for High-efficiency Dye-sensitized Solar Cells
resolves10.1016/j.ccr.2012.02.005
Cyclometalated ruthenium chromophores for the dye-sensitized solar cell
resolves10.1039/c2dt30825h
Cycloruthenated sensitizers: improving the dye-sensitized solar cell with classical inorganic chemistry principles
resolves10.1039/c2cc00136e
Three is not a crowd: efficient sensitization of TiO2 by a bulky trichromic trisheteroleptic cycloruthenated dye
resolves10.1016/j.electacta.2015.06.023
Highly efficient and stable cyclometalated ruthenium(II) complexes as sensitizers for dye-sensitized solar cells
resolves10.1021/ja9002684
New Paradigm in Molecular Engineering of Sensitizers for Solar Cell Applications
resolves10.1021/acs.inorgchem.6b00842
Ligand Engineering for the Efficient Dye-Sensitized Solar Cells with Ruthenium Sensitizers and Cobalt Electrolytes
resolves10.1039/C4TC02915A
Photostable trifluoromethyl-substituted platinum(
<scp>ii</scp>
) emitters for continuous monitoring of molecular oxygen
resolves10.1021/ic100761f
Synthesis and Characterization of Luminescent Bis-Cyclometalated Platinum<sup>IV</sup> Complexes
resolves10.1016/j.dyepig.2013.09.030
Novel triphenylamine-based cyclometalated platinum(II) complexes for efficient luminescent oxygen sensing
resolves10.1021/ic026230r
Synthesis, Characterization, and Evaluation of [Ir(ppy)<sub>2</sub>(vpy)Cl] as a Polymer-Bound Oxygen Sensor
resolves10.1039/c0jm01794a
Tuning the emission properties of cyclometalated platinum(II) complexes by intramolecular electron-sink/arylethynylated ligands and its application for enhanced luminescent oxygen sensing
resolves10.1039/a708630j
Sulfur dioxide gas detection by reversible η1-SO2–Pt bond formation as a novel application for periphery functionalised metallo-dendrimers‡
resolves10.1002/(SICI)1521-4095(199902)11:2<171::AID-ADMA171>3.0.CO;2-F
Gas Sensor Materials Based on Metallodendrimers
resolves10.1002/(SICI)1521-3765(20000417)6:8<1431::AID-CHEM1431>3.0.CO;2-D
Diagnostic Organometallic and Metallodendritic Materials for SO2 Gas Detection: Reversible Binding of Sulfur Dioxide to Arylplatinum(II) Complexes
resolves10.1039/b105660n
Detection of ppm quantities of gaseous SO2 by organoplatinum dendritic sites immobilised on a quartz microbalance
resolves10.1021/ic0009019
Mechanistic Aspects of the Reversible Binding of SO<sub>2</sub> on Arylplatinum Complexes: Experimental and ab Initio Studies
resolves10.1021/ic102082k
Ratiometric Phosphorescence Imaging of Hg(II) in Living Cells Based on a Neutral Iridium(III) Complex
resolves10.1021/ic800500c
Highly Selective Phosphorescent Chemosensor for Fluoride Based on an Iridium(III) Complex Containing Arylborane Units
resolves10.1021/ja710803p
Signal Amplification via Intramolecular Energy Transfer Using Tripodal Neutral Iridium(III) Complexes upon Binding to Avidin
resolves10.1021/ic300655x
Large Improvement in the Catalytic Activity Due to Small Changes in the Diimine Ligands: New Mechanistic Insight into the Dirhodium(II,II) Complex-Based Photocatalytic H<sub>2</sub>Production
resolves10.1021/ja0427101
Discovery and High-Throughput Screening of Heteroleptic Iridium Complexes for Photoinduced Hydrogen Production
resolves10.1021/ic800988b
Homogeneous Catalytic System for Photoinduced Hydrogen Production Utilizing Iridium and Rhodium Complexes
resolves10.1039/c0cc01827a
Robust photocatalytic water reduction with cyclometalated Ir(iii) 4-vinyl-2,2′-bipyridine complexes
resolves10.1021/ja201514e
Orchestrated Photocatalytic Water Reduction Using Surface-Adsorbing Iridium Photosensitizers
resolves10.1039/C6DT01516F
Cyano-decorated ligands: a powerful alternative to fluorination for tuning the photochemical properties of cyclometalated Ir(
<scp>iii</scp>
) complexes
resolves10.1002/chem.201203029
Charge‐Neutral Amidinate‐Containing Iridium Complexes Capable of Efficient Photocatalytic Water Reduction
resolves10.1021/ic202423y
Impact of Ligand Modification on Hydrogen Photogeneration and Light-Harvesting Applications Using Cyclometalated Iridium Complexes
resolves10.1002/aoc.1823
<i>S</i>,<i>N</i>‐Chelated organotin(IV) compounds containing 6‐phenylpyridazine‐3‐thiolate ligand—structural, antibacterial and antifungal study
resolves10.1016/j.jinorgbio.2014.07.001
Cyclopalladated and cycloplatinated benzophenone imines: Antitumor, antibacterial and antioxidant activities, DNA interaction and cathepsin B inhibition
resolves10.1016/j.jorganchem.2016.06.013
New platinum(II) complexes of CCC-pincer N-heterocyclic carbene ligand: Synthesis, characterization, cytotoxicity and antileishmanial activity
The 40 references without a DOI — listed, not checked
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib6
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib13
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib16
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib21
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib22a
no DOI — not checkedChiral pincer complexes and their application to asymmetric synthesis
no DOI — not checkedPincer complexes of N-Heterocyclic carbenes. Potential uses as pharmaceuticals
no DOI — not checkedStability of supported pincer complex-based catalysts in Heck catalysis
no DOI — not checkedDendrimers incorporating metallopincer functionalities synthesis and applications
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib23a
no DOI — not checkedC-H bond activation
no DOI — not checkedCyclopalladated compounds as resolving agents for racemic mixtures
no DOI — not checkedApplication of cyclopalladated compounds as catalysts for Heck and sonogashira reactions
no DOI — not checkedPalladacyclic pre-catalysts for Suzuki coupling, buchwald-hartwig amination and related reactions
no DOI — not checkedOther uses of palladacycles in synthesis
no DOI — not checkedCyclopalladated compounds as enzyme prototypes and anticancer drugs
no DOI — not checkedPalladcycles on dendrimers and StarShaped molecues
no DOI — not checkedLiquid crystalline ortho-palladated complexes
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib30
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib33
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib39
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib43
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib44
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib58
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib59
no DOI — not checkedR. Mertens, A Guide to OLED Technology, Industry & Market, 2014 Ed.
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib61
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib62
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib86
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib96a
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib96b
no DOI — not checkedC.K.-L. Li, R.W.-Y. Sun, S.C.-F. Kui, N. Zhu, C.-M. Che, Chem. Eur J., 12 (205253.
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib110c
no DOI — not checkedC.-M. Che, R.W.-Y. Sun, J. Yan, US Patent, US-2011/0098264 A1, 2011.
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib112
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib124
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib139
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib152
no DOI — not checkedC.P. Berlinguette, P. Bomben, WO 2012/155247A1, May 13, 2011.
no DOI — not checked10.1016/j.jorganchem.2018.05.015_bib179
What this badge says. CiteStamped means the CHECKABLE references of this
work were clean at the dated check: each resolved to a known work in a public registry, and none
carried a retraction notice at that time. It says nothing about the quality, findings,
or importance of the work itself, and nothing about references deposited without a DOI.
checked 2026-07-23 — re-checked daily as this page is visited; titles and statuses come from Crossref and DataCite and are not part of the signed record
Embed this badge
Both snippets point at the live badge image and link back to this page. The badge re-renders from the daily check, so an embed never goes stale by more than a day of visits.
<a href="https://citestamp.com/citestamped/10.1016/j.jorganchem.2018.05.015"><img src="https://citestamp.com/citestamped/10.1016/j.jorganchem.2018.05.015/badge.svg" alt="CiteStamped reference-health badge" width="460" height="64"></a>
[](https://citestamp.com/citestamped/10.1016/j.jorganchem.2018.05.015)